Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance.
- NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_assertion description "[Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance.
- NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_assertion evidence source_evidence_literature NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance.
- NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_assertion SIO_000772 15248097 NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance.
- NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_assertion wasDerivedFrom befree-2016 NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance.
- NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_assertion wasGeneratedBy ECO_0000203 NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance.
- befree-2016 importedOn "2016-02-19" NP451616.RAjRGe0p_-Saw08HrS6xflCbIua4wSILf1urS_5Ld31zE130_provenance.